Variant report

Variant	nsv1051741
Chromosome Location	chr15:34915012-35032162
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1189)
CpG islands
(count:366)
Chromatin interactive
region (count:82)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1189 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:34952157-34952158	K562	blood:	n/a	n/a
2	ARID3A	chr15:34916436-34916602	K562	blood:	n/a	n/a
3	ARID3A	chr15:34989159-34989187	K562	blood:	n/a	n/a
4	ARID3A	chr15:34946314-34948129	K562	blood:	n/a	n/a
5	ARID3A	chr15:34953056-34953951	K562	blood:	n/a	n/a
6	ARID3A	chr15:34949658-34950365	K562	blood:	n/a	n/a
7	ARID3A	chr15:34915270-34915290	K562	blood:	n/a	n/a
8	ARID3A	chr15:34944080-34945342	K562	blood:	n/a	n/a
9	ARID3A	chr15:34939172-34940883	K562	blood:	n/a	n/a
10	ARID3A	chr15:34929245-34929276	K562	blood:	n/a	n/a
11	ARID3A	chr15:34954510-34955719	K562	blood:	n/a	n/a
12	ARID3A	chr15:34948740-34948973	K562	blood:	n/a	n/a
13	ARID3A	chr15:35000570-35000896	K562	blood:	n/a	n/a
14	ATF1	chr15:34940100-34940799	K562	blood:	n/a	n/a
15	ATF1	chr15:35000572-35001097	K562	blood:	n/a	n/a
16	ATF1	chr15:34946741-34947211	K562	blood:	n/a	n/a
17	ATF1	chr15:34944877-34945255	K562	blood:	n/a	n/a
18	ATF1	chr15:34936394-34936711	K562	blood:	n/a	n/a
19	ATF1	chr15:34947575-34947975	K562	blood:	n/a	n/a
20	ATF1	chr15:35006704-35007397	K562	blood:	n/a	n/a
21	ATF1	chr15:34949656-34950320	K562	blood:	n/a	n/a
22	ATF1	chr15:34985696-34985896	K562	blood:	n/a	n/a
23	ATF1	chr15:35019827-35019831	K562	blood:	n/a	n/a
24	ATF2	chr15:34942319-34942566	GM12878	blood:	n/a	n/a
25	ATF2	chr15:34942304-34942739	GM12878	blood:	n/a	n/a
26	BACH1	chr15:34949732-34950003	K562	blood:	n/a	n/a
27	BACH1	chr15:34944497-34944500	K562	blood:	n/a	n/a
28	BATF	chr15:34942205-34942724	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449
29	BATF	chr15:34942288-34942693	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449
30	BCL11A	chr15:34942342-34942649	GM12878	blood:	n/a	n/a
31	BCL11A	chr15:34942273-34942696	GM12878	blood:	n/a	n/a
32	BCLAF1	chr15:34949675-34950412	K562	blood:	n/a	n/a
33	BCLAF1	chr15:34946604-34947084	K562	blood:	n/a	chr15:34946703-34946712
34	BHLHE40	chr15:34949672-34950063	K562	blood:	n/a	n/a
35	BHLHE40	chr15:34952400-34952527	K562	blood:	n/a	n/a
36	BHLHE40	chr15:34947721-34947910	K562	blood:	n/a	n/a
37	BHLHE40	chr15:35000622-35001023	K562	blood:	n/a	n/a
38	BHLHE40	chr15:35026609-35026748	K562	blood:	n/a	n/a
39	BHLHE40	chr15:34985524-34985579	K562	blood:	n/a	n/a
40	BHLHE40	chr15:34957939-34958132	K562	blood:	n/a	n/a
41	BHLHE40	chr15:35006695-35007250	K562	blood:	n/a	n/a
42	BHLHE40	chr15:34944964-34945198	K562	blood:	n/a	n/a
43	BHLHE40	chr15:34942322-34942647	K562	blood:	n/a	n/a
44	BRCA1	chr15:35015346-35015372	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr15:35014429-35014488	H1-hESC	embryonic stem cell:	n/a	n/a
46	BRCA1	chr15:34971598-34971907	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr15:35014096-35015138	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr15:34985718-34985922	Hela-S3	cervix:	n/a	n/a
49	CBX3	chr15:34925387-34926073	K562	blood:	n/a	n/a
50	CBX3	chr15:35000583-35000970	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:34988869-34988919	GM12891	blood:	n/a
2	chr15:35017944-35017994	MCF-7	breast:	n/a
3	chr15:35010826-35010876	K562	blood:	n/a
4	chr15:35010826-35010876	IMR90	lung:	fetal
5	chr15:35001084-35001134	HEEpiC	esophagus:	n/a
6	chr15:35001084-35001134	NHBE	bronchial:	n/a
7	chr15:34988869-34988919	BJ	skin:	n/a
8	chr15:34988869-34988919	Hepatocyte	liver:	n/a
9	chr15:35001084-35001134	AG09319	gingival:	n/a
10	chr15:34988869-34988919	GM19239	blood:	n/a
11	chr15:35001084-35001134	HepG2	liver:	n/a
12	chr15:35010826-35010876	HRCEpiC	kidney:	n/a
13	chr15:35014270-35014320	GM12878	blood:	n/a
14	chr15:35014229-35014279	ovcar-3	ovarian:	n/a
15	chr15:35010826-35010876	AoSMC	blood vessel:	n/a
16	chr15:35014229-35014279	NH-A	brain:	n/a
17	chr15:35001084-35001134	BJ	skin:	n/a
18	chr15:35001084-35001134	IMR90	lung:	fetal
19	chr15:35001084-35001134	Caco-2	colon:	n/a
20	chr15:35014270-35014320	CMK	blood:	n/a
21	chr15:35014229-35014279	SK-N-SH_RA	brain:	n/a
22	chr15:35017944-35017994	SAEC	small airway:	n/a
23	chr15:35001084-35001134	T-47D	breast:	n/a
24	chr15:35010826-35010876	GM12891	blood:	n/a
25	chr15:35014270-35014320	HCM	heart:	n/a
26	chr15:35017944-35017994	NT2-D1	testis:	n/a
27	chr15:35010826-35010876	ProgFib	skin:	n/a
28	chr15:35001084-35001134	AG10803	skin:	n/a
29	chr15:35017944-35017994	ECC-1	luminal epithelium:	n/a
30	chr15:35017944-35017994	GM12891	blood:	n/a
31	chr15:35017944-35017994	T-47D	breast:	n/a
32	chr15:35010826-35010876	ovcar-3	ovarian:	n/a
33	chr15:35001084-35001134	U87	brain:	n/a
34	chr15:35010826-35010876	NB4	blood:	n/a
35	chr15:35010826-35010876	HEK293	kidney:	embryo
36	chr15:35010826-35010876	RPTEC	kidney:	n/a
37	chr15:34988869-34988919	Hela-S3	cervix:	n/a
38	chr15:35001084-35001134	HL-60	blood:	n/a
39	chr15:35014229-35014279	SAEC	small airway:	n/a
40	chr15:35001084-35001134	ProgFib	skin:	n/a
41	chr15:35010826-35010876	NH-A	brain:	n/a
42	chr15:35010826-35010876	AG04449	skin:	fetal
43	chr15:35014229-35014279	T-47D	breast:	n/a
44	chr15:35014229-35014279	HCF	heart:	n/a
45	chr15:35014270-35014320	HPAEpiC	pulmonary alveolar:	n/a
46	chr15:35014270-35014320	PANC-1	pancreas:	n/a
47	chr15:35014270-35014320	PFSK-1	brain:	n/a
48	chr15:34988869-34988919	HUVEC	blood vessel:	n/a
49	chr15:34988869-34988919	PrEC	prostate:	n/a
50	chr15:35014229-35014279	AG04449	skin:	fetal

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:34940257..34942550-chr15:34950335..34951889,2	K562	blood:
2	chr15:34965205..34967093-chr15:34977923..34979811,2	K562	blood:
3	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
4	chr15:34965468..34967744-chr15:34968524..34970610,2	K562	blood:
5	chr15:34963103..34965254-chr15:34966851..34969218,2	MCF-7	breast:
6	chr15:35014688..35016306-chr15:35021250..35023169,2	K562	blood:
7	chr15:34960754..34962321-chr15:34966390..34968165,2	K562	blood:
8	chr10:75006642..75007633-chr15:35013735..35014638,2	Hela-S3	cervix:
9	chr15:34937548..34939695-chr15:34950801..34953012,2	K562	blood:
10	chr15:34965468..34967744-chr15:34968524..34970610,2	K562	blood:
11	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
12	chr15:34913307..34914991-chr15:34929235..34931577,2	K562	blood:
13	chr15:34965205..34967093-chr15:34977923..34979811,2	K562	blood:
14	chr15:34949722..34952645-chr15:34986997..34989606,2	K562	blood:
15	chr15:34933035..34934548-chr15:34938251..34939915,2	K562	blood:
16	chr15:34988822..34991429-chr15:34996883..34999400,2	K562	blood:
17	chr15:34983650..34987842-chr15:34989482..34992979,5	K562	blood:
18	chr15:35010787..35013754-chr15:35014491..35016542,2	K562	blood:
19	chr15:34940940..34942564-chr15:34999108..35001019,2	K562	blood:
20	chr15:34913694..34916752-chr15:34919011..34920724,3	K562	blood:
21	chr15:35010890..35011778-chr17:59321038..59321843,2	MCF-7	breast:
22	chr15:35012152..35014532-chr15:35016625..35018343,2	MCF-7	breast:
23	chr15:35020981..35022904-chr15:35025559..35027089,2	K562	blood:
24	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:
25	chr15:34965188..34969119-chr15:34970987..34974956,6	K562	blood:
26	chr15:34940940..34942564-chr15:34999108..35001019,2	K562	blood:
27	chr15:34934770..34937620-chr15:34950647..34953239,2	K562	blood:
28	chr15:34983713..34985317-chr6:26197593..26200143,2	K562	blood:
29	chr15:34949750..34952665-chr15:35241317..35244101,2	K562	blood:
30	chr15:34962434..34964585-chr15:34966364..34969710,3	K562	blood:
31	chr15:34912716..34916752-chr15:34917196..34920581,4	K562	blood:
32	chr15:34937548..34939695-chr15:34950801..34953012,2	K562	blood:
33	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:
34	chr15:35032021..35034684-chr15:35036681..35039142,3	K562	blood:
35	chr15:34907702..34910411-chr15:34952455..34954523,2	K562	blood:
36	chr15:34989332..34992979-chr15:34995533..34998034,4	K562	blood:
37	chr15:34946410..34947955-chr15:34948303..34950980,2	K562	blood:
38	chr15:34941429..34944034-chr15:34952465..34954233,2	K562	blood:
39	chr15:35005516..35008329-chr15:35009732..35011993,2	K562	blood:
40	chr15:34997005..34998827-chr15:34999088..35001652,2	K562	blood:
41	chr15:34941344..34943269-chr15:34977002..34979213,2	K562	blood:
42	chr15:34997005..34998827-chr15:34999088..35001652,2	K562	blood:
43	chr15:34934770..34937620-chr15:34950647..34953239,2	K562	blood:
44	chr15:34940257..34942550-chr15:34950335..34951889,2	K562	blood:
45	chr15:34953069..34954628-chr15:34955083..34957176,2	K562	blood:
46	chr15:34983650..34987842-chr15:34989482..34992979,5	K562	blood:
47	chr15:34941344..34943269-chr15:34977002..34979213,2	K562	blood:
48	chr15:34960754..34962321-chr15:34966390..34968165,2	K562	blood:
49	chr15:35005678..35008340-chr15:35281317..35283659,2	K562	blood:
50	chr15:35001097..35003090-chr15:35007070..35008790,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC114546.1-13	chr15:34972962-34973170	uc_385_+
2	lnc-GOLGA8A-1	chr15:34962302-34962370	XLOC_011421
3	lnc-GJD2-2	chr15:34972962-34973170	uc_385_-
4	lnc-GOLGA8A-1	chr15:34943336-34943463	ENSG00000261304.1
5	lnc-AC114546.1-4	chr15:35014395-35014438	NONHSAT041604
6	lnc-GOLGA8A-1	chr15:34943885-34943977	ENSG00000261304.1
7	lnc-GJD2-1	chr15:34967556-34967834	XLOC_011422
8	lnc-AC114546.1-4	chr15:35015809-35016397	NONHSAT041604
9	lnc-AC114546.1-4	chr15:35014273-35014438	XLOC_011205
10	lnc-GOLGA8A-1	chr15:34947820-34947978	XLOC_011421
11	lnc-AC114546.1-12	chr15:34982173-34982277	NONHSAT041602
12	lnc-AC114546.1-12	chr15:34988228-34988460	NONHSAT041602
13	lnc-AC114546.1-4	chr15:35015735-35016108	XLOC_011205
14	lnc-GOLGA8A-1	chr15:34947820-34947965	ENSG00000261304.1
15	lnc-GOLGA8A-1	chr15:34948237-34948332	ucscGeneNc_uc001zji_1
16	lnc-GJD2-1	chr15:35012518-35012708	XLOC_011422
17	lnc-GOLGA8A-1	chr15:34946499-34946618	ENSG00000261304.1
18	lnc-GOLGA8A-1	chr15:34943936-34946139	ucscGeneNc_uc001zji_1

No data

Variant related genes	Relation type
ENSG00000261304	TF binding region
ENSG00000261304	CpG island
ENSG00000197846	chromatin interactions
ENSG00000197409	chromatin interactions
ENSG00000236756	chromatin interactions
ENSG00000261304	chromatin interactions
ENSG00000196866	chromatin interactions
NEK9	miRNA target sites
NEK7	miRNA target sites

Extended variants
information (count: 4097 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:4097 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12440564	chr15:34915012-34915013	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs79432838	chr15:34915092-34915093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183211296	chr15:34915098-34915099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562328212	chr15:34915121-34915122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs148270135	chr15:34915240-34915241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376097537	chr15:34915257-34915258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547976048	chr15:34915268-34915269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560775549	chr15:34915288-34915289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs8041812	chr15:34915289-34915290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs75860786	chr15:34915298-34915299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs8036908	chr15:34915329-34915330	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs532029624	chr15:34915347-34915348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527672671	chr15:34915375-34915376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117147030	chr15:34915421-34915422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568362348	chr15:34915438-34915439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535988337	chr15:34915467-34915468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186044492	chr15:34915515-34915516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190408162	chr15:34915572-34915573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183403243	chr15:34915638-34915639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558444108	chr15:34915640-34915641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576759761	chr15:34915642-34915643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111244143	chr15:34915658-34915659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544155238	chr15:34915696-34915697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556773664	chr15:34915829-34915830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565315279	chr15:34915830-34915831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556171193	chr15:34915844-34915845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574340618	chr15:34915854-34915855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567728687	chr15:34915877-34915878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539633779	chr15:34915935-34915936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558664074	chr15:34915953-34915954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187845166	chr15:34916018-34916019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6495694	chr15:34916020-34916021	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs527908336	chr15:34916060-34916061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192753831	chr15:34916061-34916062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539543986	chr15:34916071-34916072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564650842	chr15:34916076-34916077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs8042246	chr15:34916127-34916128	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs74613284	chr15:34916129-34916130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs8042895	chr15:34916187-34916188	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs182348346	chr15:34916196-34916197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547892485	chr15:34916199-34916200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565803255	chr15:34916205-34916206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139269321	chr15:34916232-34916233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114048420	chr15:34916262-34916263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187924266	chr15:34916288-34916289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545681909	chr15:34916381-34916382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192644551	chr15:34916401-34916402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564231453	chr15:34916402-34916403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556141577	chr15:34916453-34916454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184833942	chr15:34916493-34916494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prader-willi syndrome	21504564	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:759 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34913400-34917200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr15:34914400-34916600	Weak transcription	HUVEC	blood vessel
3	chr15:34914600-34917000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr15:34915000-34918800	Weak transcription	K562	blood
5	chr15:34915600-34917000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr15:34916600-34918600	Enhancers	HUVEC	blood vessel
7	chr15:34917000-34917400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr15:34917000-34918000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr15:34917200-34917600	Enhancers	NHEK	skin
10	chr15:34917200-34917800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr15:34917400-34917600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr15:34917600-34920000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr15:34917600-34920000	Weak transcription	NHEK	skin
14	chr15:34917800-34920200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr15:34918600-34920000	Weak transcription	HUVEC	blood vessel
16	chr15:34919000-34919200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr15:34919200-34920200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr15:34920000-34920400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr15:34920000-34921600	Enhancers	NHEK	skin
20	chr15:34920000-34922200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr15:34920000-34922400	Enhancers	HUVEC	blood vessel
22	chr15:34920200-34921000	Enhancers	HMEC	breast
23	chr15:34920200-34921200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr15:34920200-34921600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr15:34920200-34921600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr15:34920400-34921200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr15:34920800-34921400	Enhancers	A549	lung
28	chr15:34920800-34921400	Enhancers	NHLF	lung
29	chr15:34921200-34921400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr15:34921200-34923000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr15:34921400-34923200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr15:34922200-34923200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr15:34923200-34923400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr15:34923200-34923400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr15:34923200-34923400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr15:34923200-34923400	Enhancers	NHEK	skin
37	chr15:34929000-34929400	Enhancers	K562	blood
38	chr15:34929400-34931400	Weak transcription	K562	blood
39	chr15:34931400-34932800	Enhancers	K562	blood
40	chr15:34932600-34932800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr15:34932800-34934400	Weak transcription	K562	blood
42	chr15:34932800-34936200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr15:34934400-34934600	Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr15:34934400-34935200	Enhancers	K562	blood
45	chr15:34934600-34934800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr15:34935200-34935800	Weak transcription	K562	blood
47	chr15:34935800-34937400	ZNF genes & repeats	K562	blood
48	chr15:34936000-34936200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr15:34936000-34937000	Enhancers	HSMM	muscle
50	chr15:34936200-34936600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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